Research Unit Lung Repair and Regeneration, Helmholtz Zentrum München, German Research Center for Environmental Health, Ludwig-Maximilians-University, University Hospital Grosshadern, Member of the German Center of Lung Research (DZL), Munich, Germany.
Lung Bioengineering and Regeneration, Department of Experimental Medical Sciences, Wallenberg Centre for Molecular Medicine, Stem Cell Center, Faculty of Medicine, Lund University, Lund, Sweden.
Eur Respir Rev. 2020 Oct 15;29(157). doi: 10.1183/16000617.0222-2020. Print 2020 Sep 30.
Most chronic and acute lung diseases have no cure, leaving lung transplantation as the only option. Recent work has improved our understanding of the endogenous regenerative capacity of the lung and has helped identification of different progenitor cell populations, as well as exploration into inducing endogenous regeneration through pharmaceutical or biological therapies. Additionally, alternative approaches that aim at replacing lung progenitor cells and their progeny through cell therapy, or whole lung tissue through bioengineering approaches, have gained increasing attention. Although impressive progress has been made, efforts at regenerating functional lung tissue are still ineffective. Chronic and acute lung diseases are most prevalent in the elderly and alterations in progenitor cells with ageing, along with an increased inflammatory milieu, present major roadblocks for regeneration. Multiple cellular mechanisms, such as cellular senescence and mitochondrial dysfunction, are aberrantly regulated in the aged and diseased lung, which impairs regeneration. Existing as well as new human models are being developed, improved and adapted in order to study potential mechanisms of lung regeneration in different contexts. This review summarises recent advances in understanding endogenous as well as exogenous regeneration and the development of models for studying regenerative mechanisms.
大多数慢性和急性肺部疾病都无法治愈,因此肺移植成为唯一的选择。最近的研究工作增进了我们对肺部内源性再生能力的理解,并有助于鉴定不同的祖细胞群体,以及探索通过药物或生物疗法来诱导内源性再生。此外,通过细胞治疗替代肺祖细胞及其后代,或通过生物工程方法替代整个肺组织的替代方法也越来越受到关注。尽管已经取得了令人瞩目的进展,但生成功能性肺组织的努力仍然效果不佳。慢性和急性肺部疾病在老年人中最为常见,祖细胞随着年龄的增长而发生变化,以及炎症环境的增加,这给再生带来了重大障碍。多种细胞机制,如细胞衰老和线粒体功能障碍,在衰老和患病的肺部中异常调节,从而损害了再生。为了研究不同背景下肺再生的潜在机制,正在开发、改进和调整现有的和新的人类模型。本综述总结了在理解内源性和外源性再生以及开发研究再生机制的模型方面的最新进展。